Teams at Tarsus Pharmaceuticals

Leads outsourced nonclinical pharmacology studies across discovery and early clinical development. Responsibilities include study planning, CRO oversight, protocol and data review, study-result interpretation, regulatory documentation, and cross-functional collaboration. The role supports in vitro and in vivo efficacy, mechanism-of-action, proof-of-concept, GLP, and non-GLP programs while maintaining scientific rigor, data integrity, and regulatory readiness.

Leads cross-functional program management for a late-stage drug development program from Phase 2b/3 through regulatory submission, approval, and launch readiness. Responsibilities include integrated planning, pivotal trial coordination, regulatory filing execution, risk and scenario planning, governance, budget and resource tracking, stakeholder alignment, and continuous improvement. The role requires extensive biotech or pharmaceutical product development experience and strong program leadership skills.

Leads pharmacokinetic, DMPK, bioanalytical, and translational PK/PD strategy across discovery through clinical development. Designs and interprets studies, guides dose selection and human PK projections, manages CROs and external partners, identifies development risks, and contributes to regulatory submissions. Partners cross-functionally on candidate evaluation, clinical planning, and governance while advancing modeling, simulation, AI-enabled methods, scientific capabilities, and team development.